DE582263C - Process for dyeing acetate silk - Google Patents

Process for dyeing acetate silk

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Publication number
DE582263C
DE582263C DEI42408D DEI0042408D DE582263C DE 582263 C DE582263 C DE 582263C DE I42408 D DEI42408 D DE I42408D DE I0042408 D DEI0042408 D DE I0042408D DE 582263 C DE582263 C DE 582263C
Authority
DE
Germany
Prior art keywords
anthrapyrimidine
amino
acetate silk
red
dyeing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
DEI42408D
Other languages
German (de)
Inventor
Dr Karl Koeberle
Dr Joachim Mueller
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to DEI42408D priority Critical patent/DE582263C/en
Application granted granted Critical
Publication of DE582263C publication Critical patent/DE582263C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B5/00Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
    • C09B5/02Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
    • C09B5/16Benz-diazabenzanthrones, e.g. anthrapyrimidones

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Description

Verfahren zum Färben von Acetatseide Es wurde gefunden, daß man klare, sehr echte und kräftige Färbungen auf Acetatseide erhält, wenn man zum Färben der Acetatseide Amino-I - 9-anthrapyrimidine oder deren Derivate verwendet. Man färbt die genannten Farbstoffe in der üblichen Weise, z. B. in Gegenwart von Dispergiermitteln, in saurem, neutralem oder alkalischem Bade. Die so erhältlichen Färbungen zeichnen sich durch besondere Lebhaftigkeit des Farbtons aus und fluoreszieren im allgemeinen. Besonders wertvoll ist weiterhin, daß eine Reihe dieser Produkte, z. B. die 4-Amino-I ₧ 9-anthrapyrimidine, grünstichig gelbe Töne liefern, wie sie mit Anthrachinonderivaten oder Anthrapyrimidon- bzw. Anthrapyridonderivaten bisher nicht zu erzielen waren. Beispie1 I 3o Teile Acetatseide werden in einer Suspension von 0,3 Teilen 4-Amino-I - 9-anthrapyrimidin in Iooo Teilen Wasser und unter Zusatz von etwa 3 Teilen Marseiller Seife Stunden lang bei 65 bis 7o° C gefärbt. Darauf wird gespült und gewaschen und in der üblichen Weise getrocknet. Die so erhältliche grünstichiggelbe Färbung zeigt stark grüne Fluoreszenz und besitzt ausgezeichnete Echtheitseigenschaften.Process for dyeing acetate silk It has been found that clear, very real and strong dyeings on acetate silk are obtained if you use the Acetate silk amino-I - 9-anthrapyrimidines or their derivatives are used. One colors the dyes mentioned in the usual manner, for. B. in the presence of dispersants, in acidic, neutral or alkaline baths. Draw the colors available in this way They are distinguished by the particular vividness of the hue and generally fluoresce. It is also particularly valuable that a number of these products, e.g. B. the 4-amino-I ₧ 9-anthrapyrimidines, deliver greenish yellow tones, like those with anthraquinone derivatives or anthrapyrimidone or anthrapyridone derivatives have not yet been achieved. Beispie1 I 30 parts of acetate silk are in a suspension of 0.3 parts of 4-amino-I 9-anthrapyrimidine in 100 parts of water and with the addition of about 3 parts of Marseilles Soap colored for hours at 65 to 70 ° C. Then it is rinsed and washed and dried in the usual way. The greenish yellow coloration obtainable in this way shows strong green fluorescence and has excellent fastness properties.

An Stelle von 4-Amino-I ₧ 9-anthrapyrimidin kann man auch 4-Methylamino-I ₧ 9-anthrapyrimidin oder das aus 4-Amino-I ₧ 9-anthrapyrimidin mit Methylalkohol in Schwefelsäure erhältliche Reaktionsprodukt, ferner 4-Amino-2-methoxy- I - 9-anthrapyrimidin, 4-Amino-5-nitro-I - 9-anthrapyrimidin, 5-y-Propanolamino-I ₧ 9-anthrapyrimidin, 4-Amino-2-methyl-I - 9-anthrapyrimidin zum Färben anwenden.Instead of 4-amino-I ₧ 9-anthrapyrimidine you can also use 4-methylamino-I ₧ 9-anthrapyrimidine or that of 4-amino-I ₧ 9-anthrapyrimidine with Methyl alcohol in sulfuric acid available reaction product, also 4-amino-2-methoxy- 1-9-anthrapyrimidine, 4-amino-5-nitro-1-9-anthrapyrimidine, 5-γ-propanolamino-I ₧ Use 9-anthrapyrimidine, 4-amino-2-methyl-I - 9-anthrapyrimidine for staining.

Beispiel e Io Teile Acetatseide werden in einer Suspension von o, I Teilen 5-Amino-I - 9-anthrapyrimidin in 3oo Teilen Wasser und unter Zugabe von etwa I Teil Seife ½ bis ¾ Stunden lang bei 6o bis 70° C gefärbt. Man verfährt weiter wie im Beispiel I angegeben und erhält eine rote Färbung von sehr guter Echtheit.Example e Io parts of acetate silk are in a suspension of o, I parts of 5-amino-1-9-anthrapyrimidine in 300 parts of water and with the addition of Dyed about 1 part of soap for ½ to ¾ hours at 6o to 70 ° C. One moves on as indicated in Example I and is given a red coloration of very good fastness.

Verwendet man an Stelle von 5-Aminoi - 9-anthrapyrimidin das 5-Methylaminoderivat, so erhält man eine rotviolette Färbung.If the 5-methylamino derivative is used instead of 5-aminoi - 9-anthrapyrimidine, this gives a red-violet coloration.

Das Py-C-chlor-4-amino-i - 9-anthrapyrimidin liefert auf Acetatseide ein reines grünstichiges Gelb.The Py-C-chloro-4-amino-i-9-anthrapyrimidine yields on acetate silk a pure greenish yellow.

Beispiel 3 In der nachstehenden Tabelle sind eine Reihe weiterer, zum Färben von Acetatseide geeigneter Aminoanthrapyrimidine sowie die damit erzielten Färbungen angegeben: Aminoanthrapyrimidinderivat Färbung auf Acetatseide 8-Amino-I₧9-anthrapyrimidin ........ .................. rot 7-Amino-I₧9-anthrapyrimidin ........................... orangerot 6-Amino-I₧9-anthrapyrimidin ........................... orangerot 4-Amino-Py-C-methyl-I ₧ 9-anthrapyrimidin . . . . . . . . . . . . ... . grüngelb mit grüner Fluoreszenz 4-Amino-2-methyl-I ₧ 9-anthrapyrimidin . . . . . . . . . . . . ....... gelb 4-Amino-Py-C-methylamino-I ₧ 9-anthrapyrimidin . . . . . . . . . . lachsrot mit intensiv oranger Fluoreszenz 4-Amino-Py-C-amino-I ₧ 9-anthrapyrimidin . . . . . . . . . . . . . . . . gelb 4-Amino-Py-C-phenoxy-I ₧ 9-anthrapyrimidin . . . . . . . . . . . . . . gelb mit grüner Fluoreszenz Durch Nitrieren von I ₧ 9-Anthrapyrimidin und Reduktion blaurot der entstandenen Nitroverbindung erhaltenes Amino- I ₧ 9-anthrapyrimidin 2-Amino-I₧9-anthrapyrimidin ........................... orange . 3-Amino-I₧9-anthrapyrimidin ........................... orange Py-C-amino-I ₧ 9-anthrapyrimidin ......................... gelb 4-Amino-Py-C-dimethylamino-I ₧ 9-anthrapyrimidin........ rosa mit oranger Fluoreszenz Aminochlor-I ₧ 9-anthrapyrimidin (aus dem Kondensations- klar rot produkt von Dichlor-I ₧ 9-anthrapyrimidin, hergestellt durch Chlorieren von 5-Chlor- I ₧ 9-anthrapyrimidin in Trichlor- Benzol mit Chlor in Gegenwart von Jod, mit p-Toluol- sulfonsäureamid durch Verseifen erhalten) Aminochlor-I ₧ 9-anthrapyrimidin (dargestellt aus dem aus orange 5-Chlor-I ₧ 9-anthrapyrimidin durch Chlorieren erhältlichen Dichlor-i # 9-anthrapyrimidin durch Erhitzen mit wäßrigem Ammoniak) Example 3 The table below shows a number of other aminoanthrapyrimidines suitable for dyeing acetate silk, as well as the colorations achieved with them: Aminoanthrapyrimidine derivative staining on acetate silk 8-Amino-I ₧ 9-anthrapyrimidine ........ .................. red 7-Amino-I ₧ 9-anthrapyrimidine ........................... orange-red 6-Amino-I ₧ 9-anthrapyrimidine ........................... orange-red 4-Amino-Py-C-methyl-I ₧ 9-anthrapyrimidine. . . . . . . . . . . . ... green-yellow with green fluorescence 4-Amino-2-methyl-I ₧ 9-anthrapyrimidine. . . . . . . . . . . . ....... yellow 4-Amino-Py-C-methylamino-I ₧ 9-anthrapyrimidine. . . . . . . . . . salmon red with intense orange fluorescence 4-Amino-Py-C-amino-I ₧ 9-anthrapyrimidine. . . . . . . . . . . . . . . . yellow 4-Amino-Py-C-phenoxy-I ₧ 9-anthrapyrimidine. . . . . . . . . . . . . . yellow with green fluorescence By nitrating I ₧ 9-anthrapyrimidine and reducing it blue-red the resulting nitro compound obtained amino I ₧ 9-anthrapyrimidine 2-Amino-I ₧ 9-anthrapyrimidine ........................... orange. 3-Amino-I ₧ 9-anthrapyrimidine ........................... orange Py-C-amino-I ₧ 9-anthrapyrimidine ......................... yellow 4-Amino-Py-C-dimethylamino-I ₧ 9-anthrapyrimidine ........ pink with orange fluorescence Aminochlor-I ₧ 9-anthrapyrimidine (from the condensation clear red product of dichloro-I ₧ 9-anthrapyrimidine, manufactured by Chlorination of 5-chloro I ₧ 9-anthrapyrimidine in trichloro Benzene with chlorine in the presence of iodine, with p-toluene- sulfonic acid amide obtained by saponification) Aminochlor-I ₧ 9-anthrapyrimidine (shown from the orange 5-chloro-I ₧ 9-anthrapyrimidine obtainable by chlorination Dichloro-i # 9-anthrapyrimidine by heating with aqueous Ammonia)

Claims (1)

PATENTANSPRUCH: Verfahren zum Färben von Acetatseide, dadurch gekennzeichnet, daß man zum Färben der Acetatseide Amino-i # 9-anthrapyrimidine oder deren Derivate verwendet.PATENT CLAIM: Process for dyeing acetate silk, characterized in that that one for dyeing the acetate silk amino-i # 9-anthrapyrimidines or their derivatives used.
DEI42408D 1931-08-27 1931-08-27 Process for dyeing acetate silk Expired DE582263C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI42408D DE582263C (en) 1931-08-27 1931-08-27 Process for dyeing acetate silk

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI42408D DE582263C (en) 1931-08-27 1931-08-27 Process for dyeing acetate silk

Publications (1)

Publication Number Publication Date
DE582263C true DE582263C (en) 1933-08-11

Family

ID=7190770

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI42408D Expired DE582263C (en) 1931-08-27 1931-08-27 Process for dyeing acetate silk

Country Status (1)

Country Link
DE (1) DE582263C (en)

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